Canonical Allele Identifier: CA386299622
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1487998
ClinVar RCV Id: RCV002008996
dbSNP Id: rs570748767
MyVariant Identifiers: chr12:g.103260416G>C (hg19) chr12:g.102866638G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866638G>C , CM000674.2:g.102866638G>C GRCh38
NC_000012.11:g.103260416G>C , CM000674.1:g.103260416G>C GRCh37
NC_000012.10:g.101784546G>C NCBI36
NG_008690.1:g.55965C>G
NG_008690.2:g.96773C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.467C>G MANE Select ENSP00000448059.1:p.Ala156Gly
ENST00000307000.7:c.452C>G ENSP00000303500.2:p.Ala151Gly
ENST00000549111.5:n.563C>G
ENST00000551988.5:n.530+10824C>G
ENST00000553106.5:c.467C>G ENSP00000448059.1:p.Ala156Gly
NM_000277.1:c.467C>G NP_000268.1:p.Ala156Gly
XM_011538422.1:c.467C>G XP_011536724.1:p.Ala156Gly
NM_000277.2:c.467C>G NP_000268.1:p.Ala156Gly
NM_001354304.1:c.467C>G NP_001341233.1:p.Ala156Gly
XM_017019370.2:c.467C>G XP_016874859.1:p.Ala156Gly
NM_000277.3:c.467C>G MANE Select NP_000268.1:p.Ala156Gly
NM_001354304.2:c.467C>G NP_001341233.1:p.Ala156Gly
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